K-number	K111245
Device name	HEARTNAVIGATOR RELEASE 1
Applicant	Philips Medical Systems Nederland B.V.
Product code	LLZ
Device class	Class II
Decision date	Jul 29, 2011
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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HEARTNAVIGATOR RELEASE 1

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